Table 6. Multivariable Cox proportional hazards regression models for 30-day mortality of patients with HAP.
Variables | Unadjusted HR (95% CI) | P value | Adjusted HR (95% CI) | P value | |
---|---|---|---|---|---|
Propensity score-matched overall patientsa | |||||
Monotherapy | 1 (ref.) | 1 (ref.) | |||
Combination therapy | 0.990 (0.672–1.460) | 0.960 | 1.646 (0.782–3.461) | 0.189 | |
Microbiologically documented patientsb | |||||
Monotherapy | 1 (ref.) | 1 (ref.) | |||
Combination therapy | 1.176 (0.640–2.159) | 0.602 | 1.594 (0.803–3.165) | 0.182 | |
Clinically documented patientsc | |||||
Monotherapy | 1 (ref.) | 1 (ref.) | |||
Combination therapy | 0.825 (0.493–1.383) | 0.466 | 0.849 (0.490–1.472) | 0.561 |
HAP = hospital-acquired pneumonia, HR = hazard ratio, CI = confidence interval, CCI = Charlson Comorbidity Index, CFS = Clinical Frailty Scale, SOFA = Sequential Organ Failure Assessment, VAP = ventilator-associated pneumonia.
aAdjusted for age, sex (male), chronic neurological disease, CCI, CFS, SOFA score, classification of infection, prior antibiotic use within 90 days, risk of aspiration, late-onset HAP, VAP, combination with glycopeptides, mechanical ventilation, renal replacement therapy, A. baumannii, Enterobacteriaceae, and P. aeruginosa.
bAdjusted for age, sex (male), chronic neurological disease, CCI, CFS, SOFA score, prior antibiotic use within 90 days, aspiration risk, late-onset HAP, VAP, combination with glycopeptides, mechanical ventilation, renal replacement therapy, A. baumannii, Enterobacteriaceae, and P. aeruginosa.
cAdjusted for age, sex (male), chronic neurological disease, CCI, CFS, SOFA score, prior antibiotic use within 90 days, aspiration risk, late-onset HAP, VAP, combination with glycopeptides, mechanical ventilation, and renal replacement therapy.